Canonical Allele Identifier: CA2782134629

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127343306_127343307insG , CM000670.2:g.127343306_127343307insG GRCh38
NC_000008.10:g.128355552_128355553insG , CM000670.1:g.128355552_128355553insG GRCh37
NC_000008.9:g.128424734_128424735insG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645438.1:c.-560+3871_-560+3872insG (POU5F1B) ENSP00000495779.1:n.-560+3871_-560+3872insG
NR_117099.1:n.457+3871_457+3872insG (CASC21)
NR_117100.1:n.1177-53247_1177-53246insC (CASC8)